Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287607Generated: October 28, 2026

Ammonium Chloride → (7-Methoxy-1-benzofuran-2-yl)methanol

https://huagongshe.com/reaction/2287607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 7-methoxy-1-benzofuran-2-carboxylateHCID 521284—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Product(7-Methoxy-1-benzofuran-2-yl)methanolHCID 11788606106.4%

Reaction Steps

A mixture of 2-ethoxycarbonyl-7-methoxybenzofuran (360 mg), lithium borohydride (36 mg) in tetrahydrofuran (4 ml) was stirred at ambient temperature overnight and then for 8 hours at 50° C. Saturated ammonium chloride solution was added to the reaction mixture, and the solution was extracted with ethyl acetate. The extract was washed with saturated ammonium chloride solution and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by flash chromatography (n-hexane-ethyl acetate) to give 2-hydroxymethyl-7-methoxybenzofuran (310 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083961
Source datasetuspto-grants-2000_07
ORD IDord-e2a09a10c2d845ab890674865b7cacec
Source noteuspto-grants-2000_07